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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719221Generated: November 2, 2026

Thioacetamide → 6-Methyl-5-(2-methyl-1,3-thiazol-4-yl)-2-oxo-1,2-dihydropyridine-3-carbonitrile

https://huagongshe.com/reaction/1719221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioacetamideHCID 2723949—
Reactant5-Bromoacetyl-1,2-dihydro-6-methyl-2-oxo-3-pyridinecarbonitrileHCID 15592166—
SolventDimethylformamideHCID 6228—
Product6-Methyl-5-(2-methyl-1,3-thiazol-4-yl)-2-oxo-1,2-dihydropyridine-3-carbonitrileHCID 280125638.2%

Reaction Steps

C-1. 1,2-Dihydro-6-methyl-5-(2-methyl-4-thiazolyl)-2-oxo-3-pyridinecarbonitrile--A mixture containing 25.4 g of 5-(bromoacetyl)-1,2-dihydro-6-methyl-2-oxo-3-pyridinecarbonitrile, 7.5 g of thioacetamide and 100 ml of dimethylformamide was heated with stirring on a steam bath for 5 hours and then concentrated on a rotary evaporator. To the residual material was added 100 ml of water and 10 ml of concentrated aqueous ammonium hydroxide. The resulting mixture was filtered and the filtrate reacidified by adding acetic acid. The solid that separated was collected, washed with water and dried, and then recrystallized from dimethylformamide to produce 8.8 g of 1,2-dihydro-6-methyl-5-(2-methyl-4-thiazolyl)-2-oxo-3-pyridinecarbonitrile, m.p. 305°-307° C. with decomposition.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04539327
Source datasetuspto-grants-1985_09
ORD IDord-35640cf82813466089cf5f21267abb63
Source noteuspto-grants-1985_09